Canonical Allele Identifier: CA357056195
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754168-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754168G>C , CM000666.2:g.67754168G>C GRCh38
NC_000004.11:g.68619886G>C , CM000666.1:g.68619886G>C GRCh37
NC_000004.10:g.68302481G>C NCBI36
NG_009293.1:g.6919C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.168C>G MANE Select ENSP00000226413.5:p.Phe56Leu
ENST00000226413.4:c.168C>G ENSP00000226413.4:p.Phe56Leu
ENST00000420975.2:c.168C>G ENSP00000397561.2:p.Phe56Leu
NM_000406.2:c.168C>G NP_000397.1:p.Phe56Leu
NM_001012763.1:c.168C>G NP_001012781.1:p.Phe56Leu
NM_000406.3:c.168C>G MANE Select NP_000397.1:p.Phe56Leu
NM_001012763.2:c.168C>G NP_001012781.1:p.Phe56Leu